Product Recalls in Nebraska
Product recalls affecting Nebraska — including food, drugs, consumer products, medical devices, and vehicles distributed to Nebraska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,548 recalls have been distributed to Nebraska in the last 12 months.
Showing 14481–14500 of 49,150 recalls
Recalled Item: GEL CONDUCTOR Recalled by DJO, LLC Due to Ultrasound gels and lotions...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Promethazine With Codeine Oral Solution Recalled by Morton Grove...
The Issue: CGMP Deviations: Potential concern with products manufactured using liquid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valproic Acid Oral Solution USP Recalled by Morton Grove Pharmaceuticals,...
The Issue: CGMP Deviations: Potential concern with products manufactured using liquid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Promethazine Syrup Plain Recalled by Morton Grove Pharmaceuticals, Inc. Due...
The Issue: CGMP Deviations: Potential concern with products manufactured using liquid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AMINOSYN II 15% An Amino Acid Injection Recalled by ICU Medical Inc Due to...
The Issue: Presence of Particulate Matter: Particulate matter identified as fibers,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glycopyrrolate Injection Recalled by Meitheal Pharmaceuticals Inc Due to...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: cobas EGFR Mutation Test v2-Somatic gene mutation detection system Catalog...
The Issue: False Mutation Detected results for the exon 20 insertion (Ex20Ins) mutation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flower E-Kit Recalled by Flower Orthopedics Corporation Due to Product kit...
The Issue: Product kit missing CDG 200 (Cannulated Countersink for 3.0-4.5mm Screws)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELI Recalled by Welch Allyn Inc Mortara Due to The devices malfunction under...
The Issue: The devices malfunction under specific operator workflows.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSX0030H Recalled by W L Gore & Associates, Inc. Due to...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSX0025A Recalled by W L Gore & Associates, Inc. Due to...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSXE0030 Recalled by W L Gore & Associates, Inc. Due to...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSX0020A Recalled by W L Gore & Associates, Inc. Due to...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSXE0025B Recalled by W L Gore & Associates, Inc. Due...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSXE0030B Recalled by W L Gore & Associates, Inc. Due...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSXE0020 Recalled by W L Gore & Associates, Inc. Due to...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSX0030A Recalled by W L Gore & Associates, Inc. Due to...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSXE0025 Recalled by W L Gore & Associates, Inc. Due to...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m SARS-CoV-2 Amp Kit (Non-US Assay) and Alinity m Recalled by Abbott...
The Issue: There is a potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA Versions: 4.7 Recalled by BioMerieux SA Due to Under certain...
The Issue: Under certain conditions, there is a risk for a false negative result.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.